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白细胞介素-10-1082 启动子多态性与印度南部人群缺血性卒中风险的关系。

Interleukin-10-1082 promoter polymorphism and ischemic stroke risk in a South Indian population.

机构信息

Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad, India.

出版信息

Cytokine. 2010 Dec;52(3):221-4. doi: 10.1016/j.cyto.2010.09.013. Epub 2010 Oct 27.

Abstract

Within the past few years there has been increasing evidence that the genetic variation in the genes coding pro- and anti-inflammatory markers may play an important role in the pathogenesis of various human diseases, including stroke. The aim of the study was to evaluate the association of Interleukin-10 (IL-10)-1082 G/A, promoter polymorphism (rs1800896) with ischemic stroke in a South Indian population from Andhra Pradesh. In this study 480 ischemic stroke patients and 470 age and sex matched healthy controls were included. The ischemic stroke patients were classified according to TOAST classification. The region of interest in the IL-10 gene was amplified by polymerase chain reaction with the use of allele specific oligonucleotide primers flanking the polymorphic region. Association between genotypes and stroke was examined by Odds Ratio (OR) with 95% confidence interval (CI) and Chi-square analysis. Significant difference was observed between the patients and healthy controls, in genotypic distribution as well as allelic frequency (p<0.05). Multiple logistic regression analysis with forward stepwise selection using the potential confounders (sex, age, diabetes, hypertension, smoking and alcoholism) and IL-10 gene variant revealed that -1082 G/A polymorphism in the promoter region of IL-10 gene is significantly [adjusted OR=2.26; 95% C.I. (1.24-4.15), p<0.001] associated with ischemic stroke in the South Indian population from Andhra Pradesh. We found significant association of this polymorphism with stroke of undetermined etiology (p<0.001). Moreover, hypertensive and diabetic individuals bearing A allele of IL-10 gene in high frequency were found to be more predisposed to stroke.

摘要

在过去的几年中,越来越多的证据表明,编码前炎症和抗炎标志物的基因中的遗传变异可能在包括中风在内的各种人类疾病的发病机制中发挥重要作用。本研究旨在评估白细胞介素-10(IL-10)-1082 G/A、启动子多态性(rs1800896)与来自安得拉邦的南印度人群中缺血性中风的关联。在这项研究中,纳入了 480 名缺血性中风患者和 470 名年龄和性别匹配的健康对照者。根据 TOAST 分类,将缺血性中风患者进行分类。使用侧翼多态性区域的等位基因特异性寡核苷酸引物,通过聚合酶链反应扩增 IL-10 基因的感兴趣区域。通过优势比(OR)和 95%置信区间(CI)和卡方分析检查基因型与中风之间的关联。在患者和健康对照组之间观察到基因型分布和等位基因频率之间存在显著差异(p<0.05)。使用潜在混杂因素(性别、年龄、糖尿病、高血压、吸烟和酗酒)和 IL-10 基因变异的向前逐步选择进行多元逻辑回归分析表明,IL-10 基因启动子区域的-1082 G/A 多态性与安得拉邦的南印度人群中的缺血性中风显著相关[调整后的 OR=2.26;95%CI(1.24-4.15),p<0.001]。我们发现该多态性与未确定病因的中风显著相关(p<0.001)。此外,高频携带 IL-10 基因 A 等位基因的高血压和糖尿病个体更容易发生中风。

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